Please choose an event type to view the corresponding MedsFacts report:

DEATH ( 98 FDA reports)
DYSPNOEA ( 90 FDA reports)
RIGHT VENTRICULAR FAILURE ( 83 FDA reports)
CARDIAC FAILURE ( 62 FDA reports)
OEDEMA PERIPHERAL ( 52 FDA reports)
ANAEMIA ( 45 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 39 FDA reports)
OEDEMA ( 38 FDA reports)
HAEMOPTYSIS ( 36 FDA reports)
PNEUMONIA ( 34 FDA reports)
PULMONARY HYPERTENSION ( 34 FDA reports)
DIZZINESS ( 33 FDA reports)
HYPOXIA ( 31 FDA reports)
RESPIRATORY FAILURE ( 30 FDA reports)
DIARRHOEA ( 26 FDA reports)
NAUSEA ( 26 FDA reports)
CARDIAC ARREST ( 25 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 25 FDA reports)
PLEURAL EFFUSION ( 24 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 24 FDA reports)
FLUID RETENTION ( 23 FDA reports)
HEPATIC ENZYME INCREASED ( 23 FDA reports)
HYPOTENSION ( 23 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
RENAL FAILURE ( 22 FDA reports)
HEADACHE ( 21 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 20 FDA reports)
PALPITATIONS ( 20 FDA reports)
SYNCOPE ( 20 FDA reports)
TREMOR ( 20 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
EPISTAXIS ( 19 FDA reports)
FATIGUE ( 18 FDA reports)
RENAL IMPAIRMENT ( 18 FDA reports)
WEIGHT INCREASED ( 18 FDA reports)
CHEST PAIN ( 17 FDA reports)
FLUSHING ( 17 FDA reports)
INTERSTITIAL LUNG DISEASE ( 17 FDA reports)
ASTHENIA ( 16 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
PULMONARY OEDEMA ( 16 FDA reports)
PYREXIA ( 16 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 15 FDA reports)
TRANSAMINASES INCREASED ( 15 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
PNEUMONITIS ( 14 FDA reports)
PREGNANCY ( 14 FDA reports)
ABORTION INDUCED ( 13 FDA reports)
CELLULITIS ( 13 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 13 FDA reports)
DEHYDRATION ( 13 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 13 FDA reports)
ASCITES ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
CEREBELLAR SYNDROME ( 12 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
GAIT DISTURBANCE ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
VOMITING ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 11 FDA reports)
HEPATITIS ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
ATRIAL FLUTTER ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
HEPATIC FAILURE ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
ANURIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
CEREBELLAR ATAXIA ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
MALAISE ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
BRONCHIECTASIS ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
PNEUMOTHORAX ( 8 FDA reports)
PRESYNCOPE ( 8 FDA reports)
RASH ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
VISUAL IMPAIRMENT ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
COUGH ( 7 FDA reports)
FACE OEDEMA ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUSCLE TIGHTNESS ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CHAPPED LIPS ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
GALLBLADDER PAIN ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
INTRA-UTERINE DEATH ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LOWER LIMB FRACTURE ( 6 FDA reports)
MUCOSAL DRYNESS ( 6 FDA reports)
NASAL DRYNESS ( 6 FDA reports)
NEPHROLITHIASIS ( 6 FDA reports)
PAST-POINTING ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
FALL ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HYPOCHROMIC ANAEMIA ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACIDOSIS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BREAST CANCER STAGE IV ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PAIN ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VENTILATION PERFUSION MISMATCH ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUNG TRANSPLANT ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SUBACUTE HEPATIC FAILURE ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SYSTEMIC SCLEROSIS ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEVICE ISSUE ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYDRAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERTRANSAMINASAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PURPURA ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL EXPLORATION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ALTERNARIA INFECTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY VEIN OCCLUSION ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)

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